Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:72354886-72355226 | Common:2; Rare:121 | ||||
chr10:73096804-73096986 | Common:3; Rare:57 | ||||
chr10:73167944-73168131 | Rare:49 | ||||
chr10:73252557-73252789 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73414016-73414179 | Common:3; Rare:47 | ||||
chr10:73495618-73495762 | Rare:27 | ||||
chr10:73625983-73626118 | Rare:25 | ||||
chr10:73744247-73744430 | Common:1; Rare:48 | ||||
chr10:73772490-73772708 | Rare:97 | ||||
chr10:73772909-73773165 | Common:1; Rare:91 | ||||
chr10:73781988-73782115 | Common:1; Rare:45 | ||||
chr10:73874485-73874782 | Rare:80 | ||||
chr10:73997761-73998193 | Common:2; Rare:113 | ||||
chr10:73998272-73998303 | Rare:5; Clinvar (benign):1 | ||||
chr10:74150771-74151229 | Common:2; Rare:103 |